09/22/2021 | News release | Archived content
September 22, 2021
As a professional society representing more than 16,000 nuclear medicine professionals, it is our responsibility to ensure the health and safety of our patients and members by distributing recommendations to mitigate the risk of COVID-19 transmission in clinical practice. We understand the often-overlapping symptoms that COVID-19 and pulmonary embolism can present and appreciate the diagnostic importance of the ventilation portion of the ventilation/perfusion (V/Q) scan for patient care.
On March 19, 2020, SNMMI released a statement responding to concerns regarding V/Q lung scans and, specifically, the inherent risk of spread of COVID-19 to patients and staff related to the ventilation portion of the study. At that time, many institutions opted not to perform ventilation studies.
Subsequently, on September 3, 2020, SNMMI released an updated statement noting that since March 2020, the COVID-19 pandemic had evolved differently in various regions of the world and, with increased availability of COVID-19 PCR testing, resumption of ventilation studies could be considered in some scenarios.
Since the time of the revised statement (September 2020), there have been significant developments regarding the COVID-19 pandemic, including but not limited to emergency approval of three vaccines by the FDA, all of which are actively being distributed, and readily available COVID-19 testing for the public. Additionally, further safety measures have been introduced and implemented specific to the performance of V/Q scans.
Considering the above observations, SNMMI has again revised this statement to continue to provide the most up-to-date information to our members. SNMMI believes that ventilation scans can be increasingly incorporated as a routine part of the work-up of suspected pulmonary embolism. SNMMI recognizes that there are variations in practice patterns where the primary reliance is on perfusion-only lung scans, aided as necessary with SPECT or SPECT/CT.
The goal of this updated statement is to recognize that, in many situations, a ventilation study may be thought to be clinically necessary to help diagnose lung disease, including vascular and airway disease.In these settings, performance of ventilation studies may be considered, with local and institutional COVID-19 policies and procedures for aerosol-generating and non-aerosolizing procedures serving as the primary source of guidance.
The following considerations, which typically are included in facility policies and procedures, should be reviewed prior to performing ventilation studies:
As the incidence and the prevalence of COVID-19 vary from time to time and region to region, it may be appropriate to follow your institutional/local regulatory guidelines to determine feasibility of a ventilation scan as part of the lung scan in the work up of a suspected pulmonary embolism. SNMMI will continue to monitor the COVID-19 pandemic and provide updated information whenever possible.
References and Safety Recommendations
In addition to these considerations, the following safety updates and enhancements have been developed which may assist with specific V/Q study questions.
AMICI seeks to provide products and services that meet or exceed our customer expectations, and to continually improve the effectiveness of the Quality Management System.
The links below provide additional resources regarding quality and safety measures:
Biodex has worked urgently to provide tools to the nuclear medicine committee. The following are resources developed by Biodex in response to the COVID-19 pandemic.
|There are a variety of safeguards when using the Xenotron™ I Xenon (Xe-133) Gas Dispenser for use with xenon Xe-133 gas in Curium unit dose vials that help ensure patient safety. For more information, please visit the Curium website.|
Jubilant Radiopharma supports the SNMMI guidelines. We encourage users of DRAXIMAGE® DTPA (kit for the preparation of Technetium Tc-99m pentetate injection) to contact their preferred nebulizer supplier for the most current guidance on the safe administration of DTPA.
Click here for full prescribing information for DRAXIMAGE® MAA (kit for the preparation of technetium Tc-99m albumin aggregated injection).
Click here for DRAXIMAGE® DTPA (kit for the preparation of technetium Tc-99m pentetate injection) for intravenous and inhalation use.Click here to learn more about our pulmonary education programs.
|Lantheus is pleased to support the SNMMI's updated ventilation/perfusion (V/Q) guidance. Lantheus invites you to visit our website for comprehensive information on our xenon Xe-133 gas and our exclusive xenon Xe-133 gas Calidose® dispenser. While on our website, please view our video recognizing 50 years as the longest, continuous xenon Xe-133 gas supplier, which would not be possible without all your support.|
For over 40 years, Medi/Nuclear® has focused exclusively on image quality using radioaerosol and xenon, product safety, and customer care. Here to support the needs of nuclear departments, the following materials were created to provide practical information for enhancing safety during the COVID-19 crisis.Safer Aerosol Drug Delivery for Ventilation Studies and Respiratory Care